HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72571Generated: October 26, 2026
5-Bromo-2-chlorobenzoyl chloride → 1-[6-(5-Bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
https://huagongshe.com/reaction/72571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromo-2-chlorobenzoyl chloride | HCID 2756871 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 15171868 | HCID 15171868 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[6-(5-Bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone | HCID 86655197 | — |
Reaction Steps
To an ice cooled solution of 5-bromo-2-chlorobenzoyl chloride in dichloromethane (35 mL) was added 1-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-2,2,2-trifluoro-ethanone (6.5 g, 28.1 mmol) in dichloromethane (45 mL) followed by AlCl3 (5.61 g, 42.2 mmol) portion wise. After 2 h, the reaction mixture was brought to room temperature and stirred overnight. The reaction was quenched by pouring it over crushed ice. The resulting mixture was extracted with dichloromethane. The organic layer was washed with aq. NaHCO3 (100 mL) and water (100 mL), and the solvent was evaporated to yield the crude product which was recrystallized from hot ethylacetate to furnish 1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone (10.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08828951B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-989649abcefc4b8a9102d99a8a2c308c |
|---|
| Source note | uspto-grants-2014_09 |
|---|